A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570498



Internal ID20943569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135525669..135531742hg38UCSC Ensembl
chr9:138417515..138423588hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg386074
hg196074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280147
Samples
Known GenesLCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570498
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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